| The exosome journey: from biogenesis to uptake and intracellular signalling S Gurung, D Perocheau, L Touramanidou, J Baruteau Cell Communication and Signaling 19 (1), 47, 2021 | 818 | 2021 |
| Transcatheter closure of patent ductus arteriosus: past, present and future AE Baruteau, S Hascoët, J Baruteau, Y Boudjemline, V Lambert, ... Archives of cardiovascular diseases 107 (2), 122-132, 2014 | 187 | 2014 |
| Gene therapy for monogenic liver diseases: clinical successes, current challenges and future prospects J Baruteau, SN Waddington, IE Alexander, P Gissen Journal of inherited metabolic disease 40 (4), 497-517, 2017 | 123 | 2017 |
| cGAS-mediated induction of type I interferon due to inborn errors of histone pre-mRNA processing C Uggenti, A Lepelley, M Depp, AP Badrock, MP Rodero, MT El-Daher, ... Nature Genetics 52 (12), 1364-1372, 2020 | 120 | 2020 |
| Miglustat therapy in the French cohort of paediatric patients with Niemann-Pick disease type C B Héron, V Valayannopoulos, J Baruteau, B Chabrol, H Ogier, P Latour, ... Orphanet Journal of Rare Diseases 7, 1-14, 2012 | 117 | 2012 |
| Clinical and biological features at diagnosis in mitochondrial fatty acid beta‐oxidation defects: a French pediatric study of 187 patients J Baruteau, P Sachs, P Broué, M Brivet, H Abdoul, C Vianey‐Saban, ... Journal of Inherited Metabolic Disease: Official Journal of the Society for …, 2013 | 108 | 2013 |
| Clinical applications for exosomes: Are we there yet? D Perocheau, L Touramanidou, S Gurung, P Gissen, J Baruteau British journal of pharmacology 178 (12), 2375-2392, 2021 | 69 | 2021 |
| RAB23 mutation in a large family from Comoros Islands with Carpenter syndrome JL Alessandri, N Dagoneau, JM Laville, J Baruteau, JC Hébert, ... American Journal of Medical Genetics Part A 152 (4), 982-986, 2010 | 63 | 2010 |
| Age-related seroprevalence of antibodies against AAV-LK03 in a UK population cohort DP Perocheau, SC Cunningham, J Lee, J Antinao Diaz, SN Waddington, ... Human gene therapy 30 (1), 79-87, 2019 | 61 | 2019 |
| Expanding the phenotype in argininosuccinic aciduria: need for new therapies J Baruteau, E Jameson, AA Morris, A Chakrapani, S Santra, S Vijay, ... Journal of Inherited Metabolic Disease: Official Journal of the Society for …, 2017 | 61 | 2017 |
| Ascending vaginal infection using bioluminescent bacteria evokes intrauterine inflammation, preterm birth, and neonatal brain injury in pregnant mice N Suff, R Karda, JA Diaz, J Ng, J Baruteau, D Perocheau, M Tangney, ... The American journal of pathology 188 (10), 2164-2176, 2018 | 59 | 2018 |
| Dietary management of urea cycle disorders: European practice S Adam, MF Almeida, M Assoun, J Baruteau, SM Bernabei, S Bigot, ... Molecular genetics and metabolism 110 (4), 439-445, 2013 | 59 | 2013 |
| Neonatal hemochromatosis: diagnostic work-up based on a series of 56 cases of fetal death and neonatal liver failure S Heissat, S Collardeau-Frachon, J Baruteau, E Dubruc, R Bouvier, ... The Journal of Pediatrics 166 (1), 66-73, 2015 | 50 | 2015 |
| Successful reversal of propionic acidaemia associated cardiomyopathy: evidence for low myocardial coenzyme Q10 status and secondary mitochondrial dysfunction as an underlying … J Baruteau, I Hargreaves, S Krywawych, A Chalasani, JM Land, ... Mitochondrion 17, 150-156, 2014 | 48 | 2014 |
| Carglumic acid enhances rapid ammonia detoxification in classical organic acidurias with a favourable risk-benefit profile: a retrospective observational study V Valayannopoulos, J Baruteau, MB Delgado, A Cano, ML Couce, ... Orphanet journal of rare diseases 11, 1-11, 2016 | 47 | 2016 |
| Clinical and biological features at diagnosis in mitochondrial fatty acid beta-oxidation defects: a French pediatric study from 187 patients. Complementary data J Baruteau, P Sachs, P Broué, M Brivet, H Abdoul, C Vianey-Saban, ... Journal of inherited metabolic disease 37, 137-139, 2014 | 45 | 2014 |
| Argininosuccinic aciduria fosters neuronal nitrosative stress reversed by Asl gene transfer J Baruteau, DP Perocheau, J Hanley, M Lorvellec, E Rocha-Ferreira, ... Nature Communications 9 (1), 3505, 2018 | 44 | 2018 |
| Transient fulminant liver failure as an initial presentation in citrullinemia type I H Faghfoury, J Baruteau, HO de Baulny, J Häberle, A Schulze Molecular Genetics and Metabolism 102 (4), 413-417, 2011 | 41 | 2011 |
| Argininosuccinic aciduria: recent pathophysiological insights and therapeutic prospects J Baruteau, C Diez‐Fernandez, S Lerner, G Ranucci, P Gissen, ... Journal of inherited metabolic disease 42 (6), 1147-1161, 2019 | 39 | 2019 |
| Novel therapies for mucopolysaccharidosis type III B Seker Yilmaz, J Davison, SA Jones, J Baruteau Journal of inherited metabolic disease 44 (1), 129-147, 2021 | 38 | 2021 |
